- CTD Dossier Drafting (Modules 2, 3, 4)- Regulatory writing- Clinical Regulatory Pharmacovigilance Regulatory- Preparation of Tox applications, CTAs, MAAs
Master and CTD Dossier Drafting Review (Modules 2, 3, 4)- Preparation of Module 1 documents- Preparation and Positioning of Country specific dossiers
Professional with 3 - 6 years of experience in Internal Audit and Internal Financial Controls compliance preferably from Pharma / FMCG B2B / MFG industry and working knoweldge in ERP (SAP) e...
Lead and support in hosting all external or internal regulatory, customer, partner audits.
Develop process and plans for electronic database developmentCreate mock CRF and reveiew of EDC setup activitiesExecuting software development lifecycle
- To Drive Mega brand Growth and Performance- Optimize Promo spend for Desired ROI- Prepare Brand Wise Quarterly Visual Aid:
The candidate will play an important role in execution of various compliance audits as per the annual audit plan and ombudsperson investigations as per the Ombudsperson Policy and Procedure...
The Legal Counsel shall support and advise the business teams of GG India on its varied activities in the distribution of our expanding portfolio including our newer suite of offerings under...
Required trained/experienced in Environmental monitoringShould be trained/experienced in Water samplingShould be Graduate minimumShould be good in GMP practices and documentation skill...
Self Starter, Highly motivated Scientist, excellent written and oral skillsShould be able to supervise method development, method qualification and sample anlysis for 2-3 assets in regulat...
1. Lead the One of the Upstream manufacturing team ( Cell Culture Manufacturing Plant)and oversee the implementation of production schedules.2. Production of mammalian cell culture product...
Work experience and qualification knowledge on Compression and capsule filling machines, FBD, FBEs and coating machines, RMGs, planetary mixers, Blenders and Blisters bottle packing lines.K...